Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 110485672 | 11048567 | 2 | F | 2016 | 20160805 | 20150420 | 20160819 | EXP | CA-ABBVIE-15K-028-1376339-00 | ABBVIE | 0.00 | F | Y | 49.49000 | KG | 20160819 | CN | COUNTRY NOT SPECIFIED | CA |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 110485672 | 11048567 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | QOW | ||||||
| 110485672 | 11048567 | 2 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | QOW | ||||||
| 110485672 | 11048567 | 3 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 | ||||||||||||
| 110485672 | 11048567 | 4 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 | ||||||||||||
| 110485672 | 11048567 | 5 | C | EFFEXOR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 0 | 75 | MG | QD | ||||||||
| 110485672 | 11048567 | 6 | C | FOLIC ACID. | FOLIC ACID | 1 | 0 | ||||||||||||
| 110485672 | 11048567 | 7 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 110485672 | 11048567 | 1 | Crohn's disease |
| 110485672 | 11048567 | 3 | Crohn's disease |
| 110485672 | 11048567 | 4 | Arthritis |
| 110485672 | 11048567 | 5 | Antidepressant therapy |
| 110485672 | 11048567 | 6 | Crohn's disease |
| 110485672 | 11048567 | 7 | Crohn's disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 110485672 | 11048567 | OT |
| 110485672 | 11048567 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 110485672 | 11048567 | Abdominal adhesions | |
| 110485672 | 11048567 | Decubitus ulcer | |
| 110485672 | 11048567 | Gastrointestinal obstruction | |
| 110485672 | 11048567 | Intestinal obstruction | |
| 110485672 | 11048567 | Intestinal stenosis | |
| 110485672 | 11048567 | Post procedural discomfort | |
| 110485672 | 11048567 | Skin disorder |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 110485672 | 11048567 | 1 | 20101027 | 20160614 | 0 | |
| 110485672 | 11048567 | 2 | 2016 | 0 |